Director of Quality

The company is a leading International cGMP Contract Development and Manufacturing Organisation (CDMO) supporting the global life sciences industry in the development and manufacture of DNA, viral vectors, microbiota, proteins and pharmaceuticals for clinical trials and commercial supply.

They provide a comprehensive biologics and pharmaceuticals service offering, with multi-functional and experienced Advanced Therapies project teams nurturing customers’ plasmid DNA, viral vector and microbiota products from pre-clinical through to clinical and commercial manufacture within GMP approved facilities.

A Director of Quality is required to take responsibility for the Quality Control and Quality Assurance Teams with a headcount of c40 people, supported by contract QP’s.

  • To be responsible for the site Quality Group ensuring that operational activities are GMP compliant within the MHRA guidelines and that activities are coordinated to meet customer deliverables alongside the Operations and Commercial Groups.
  • To lead on all GMP related matters for the site as well as being the prime point of contact with customers with respect to GMP and quality matters.

They have two GMP approved facilities, located in the UK and Europe and are planning to develop a further site shortly in the UK. These sites offer a comprehensive service to nurture projects from conception to fill and finish.

As part of a larger Group, with 100 sites globally, biologics is a key focus and they are investing heavily in the company to facilitate growth. Future prospects across the Group are exceptional.

To apply, please forward your CV to lifescience@chestertongray.com

Reference 880248